Clinical and research tests for VEGFC - Genetic Testing Registry (GTR) - NCBI

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Tests names and labs	Conditions	Genes, analytes, and microbes	Methods
Lymphedema, hereditary, ID, 615907, Autosomal dominant; LMPH1D (Milroy disease) (VEGFC gene) (Sequence Analysis-All Coding Exons) (Postnatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey	1	1	C Sequence analysis of the entire coding region
Lymphedema, hereditary, ID, 615907, Autosomal dominant; LMPH1D (Milroy disease) (VEGFC gene) (Sequence Analysis-All Coding Exons) (Prenatal) Intergen Intergen Genetics and Rare Diseases Diagnosis Center Turkey	1	1	C Sequence analysis of the entire coding region
Lymphedema Panel PreventionGenetics, part of Exact Sciences United States	15	14	D Deletion/duplication analysis C Sequence analysis of the entire coding region T Targeted variant analysis
Vascular Malformations Panel, Sequencing and Deletion/Duplication ARUP Laboratories, Molecular Genetics and Genomics ARUP Laboratories United States	24	28	D Deletion/duplication analysis C Sequence analysis of the entire coding region
Vascular Anomalies Panel with interpretation Clinical Genomics Laboratory Washington University in St. Louis United States	1	65	C Sequence analysis of the entire coding region
Lymphedema hereditary (WES based NGS panel of 22 genes, including CNV analysis) CGC Genetics Unilabs Portugal	1	22	C Sequence analysis of the entire coding region
Dermatology Panel CGC Genetics Unilabs Portugal	1	277	C Sequence analysis of the entire coding region
Lymphedema hereditary, IA (sequence analysis of VEGFC gene) CGC Genetics Unilabs Portugal	1	1	C Sequence analysis of the entire coding region
Lymphatic malformation 4 Laboratory for Molecular Diagnostics Center for Nephrology and Metabolic Disorders Germany	1	1	C Sequence analysis of the entire coding region
Genomic Unity® Custom Analysis Variantyx, Inc. United States	1	4054	D Deletion/duplication analysis X Mutation scanning of select exons C Sequence analysis of the entire coding region
Lymphedema Sequencing Panel Seattle Children's Hospital Genetics Laboratories Seattle Children's United States	29	25	C Sequence analysis of the entire coding region
Vascular Anomalies (VANseq) Expanded Del/Dup Panel Seattle Children's Hospital Genetics Laboratories Seattle Children's United States	50	47	D Deletion/duplication analysis
Vascular Anomalies (VANseq) Expanded Sequencing Panel Seattle Children's Hospital Genetics Laboratories Seattle Children's United States	50	47	C Sequence analysis of the entire coding region
NewbornDx Advanced Sequencing Evaluation Athena Diagnostics Inc United States	1	1722	C Sequence analysis of the entire coding region
Lymphatic malformation: Full gene sequencing panel CEN4GEN Institute for Genomics and Molecular Diagnostics Canada	5	5	C Sequence analysis of the entire coding region
MILROY SYNDROME SANGER PANEL Laboratorio de Genetica Clinica SL Spain	1	3	C Sequence analysis of the entire coding region
MILROY SYNDROME Laboratorio de Genetica Clinica SL Spain	2	3	X Mutation scanning of select exons E Sequence analysis of select exons
Lymphedema-Lethal Restrictive Dermopathy , Panel Massive Sequencing (NGS) 7 Genes Reference Laboratory Genetics Spain	8	7	C Sequence analysis of the entire coding region
Vascular Malformation NGS Panel Greenwood Genetic Center Diagnostic Laboratories Greenwood Genetic Center United States	34	21	C Sequence analysis of the entire coding region
VEGFC Single Gene Fulgent Genetics United States	3	1	D Deletion/duplication analysis C Sequence analysis of the entire coding region

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